Canonical Allele Identifier: CA399478098

Gene: KRT14

Linked Data

• MyVariant Identifiers: chr17:g.39740567T>A (hg19) ; chr17:g.41584315T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584315T>A , CM000679.2:g.41584315T>A	GRCh38
NC_000017.10:g.39740567T>A , CM000679.1:g.39740567T>A	GRCh37
NC_000017.9:g.36994093T>A	NCBI36
NG_008624.1:g.7581A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.707A>T MANE Select	ENSP00000167586.6:p.Glu236Val
ENST00000167586.6:c.707A>T	ENSP00000167586.6:p.Glu236Val
ENST00000476662.1:n.157A>T
NM_000526.4:c.707A>T	NP_000517.2:p.Glu236Val
NM_000526.5:c.707A>T MANE Select	NP_000517.3:p.Glu236Val